N/A - BIOMET MICROFIXATION, INC

Duns Number:046189866

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More Product Details

Catalog Number

09-0231

Brand Name

N/A

Version/Model Number

09-0231

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

HTF

Product Code Name

CURETTE

Device Record Status

Public Device Record Key

e168a5e3-eced-4fc5-9946-9ba6e5b5be09

Public Version Date

May 07, 2019

Public Version Number

2

DI Record Publish Date

August 22, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BIOMET MICROFIXATION, INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1783
2 A medical device with a moderate to high risk that requires special controls. 11874
3 A medical device with high risk that requires premarket approval 34